Pegdinetanib

From WikiMD's Wellness Encyclopedia

Pegdinetanib non-peptide structure.svg

Pegdinetanib is a biopharmaceutical drug that functions as an anti-angiogenic agent. It is a pegylated form of a recombinant human monoclonal antibody designed to inhibit the activity of vascular endothelial growth factor (VEGF), a key molecule involved in the process of angiogenesis.

Mechanism of Action[edit | edit source]

Pegdinetanib works by binding to VEGF, thereby preventing it from interacting with its receptors on the surface of endothelial cells. This inhibition disrupts the signaling pathways that promote the growth of new blood vessels, a process critical for the growth and metastasis of tumors. By blocking angiogenesis, pegdinetanib can effectively starve tumors of the necessary blood supply, inhibiting their growth and spread.

Clinical Applications[edit | edit source]

Pegdinetanib has been investigated for its potential use in the treatment of various types of cancer, including colorectal cancer, non-small cell lung cancer, and glioblastoma. Clinical trials have explored its efficacy both as a monotherapy and in combination with other chemotherapeutic agents.

Pharmacokinetics[edit | edit source]

The pegylation of dinetanib enhances its pharmacokinetic properties by increasing its half-life and reducing its immunogenicity. This modification allows for less frequent dosing and potentially improves patient compliance.

Side Effects[edit | edit source]

Common side effects associated with pegdinetanib include hypertension, proteinuria, and gastrointestinal disturbances. More severe adverse effects can include thromboembolic events and hemorrhage.

Regulatory Status[edit | edit source]

As of the latest updates, pegdinetanib is still under investigation and has not yet received approval from major regulatory bodies such as the Food and Drug Administration (FDA) or the European Medicines Agency (EMA).

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


Contributors: Prab R. Tumpati, MD